SU1327780A3 - Method of fighting weeds - Google Patents
Method of fighting weeds Download PDFInfo
- Publication number
- SU1327780A3 SU1327780A3 SU843831924A SU3831924A SU1327780A3 SU 1327780 A3 SU1327780 A3 SU 1327780A3 SU 843831924 A SU843831924 A SU 843831924A SU 3831924 A SU3831924 A SU 3831924A SU 1327780 A3 SU1327780 A3 SU 1327780A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- propyl
- millet
- compound
- herbicidal effect
- methoxy
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/81—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C233/11—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Изобретение относитс к химическим способам борьбы с сорной и нежелательной растительностью. С целью повьппени гербицидного действи в ка , честве активного вещества используют производные фенилацетанилида общей формулы Y-CjH C(CHj)(C2H5)C(0) (JP) , где У - метил, метилокси, пропилокси,трифторметил, фтор; R - С,-Сз-апкил. При использовании указанных соединений в дозах 0,3125-5 кг/га достигаетс практически полное поражение сорных растений при отсутствии фитотоксичности по отношению к куль- турным растени м, например к рису. 2 табл. СО ыThe invention relates to chemical methods for controlling weeds and unwanted vegetation. In order to increase the herbicidal action, phenylacetanilide derivatives of the general formula Y-CjH C(CHj)(C2H5)C(0) (JP) are used as the active substance, where Y is methyl, methyloxy, propyloxy, trifluoromethyl, fluorine; R - C,-C3-apkyl. When using these compounds at doses of 0.3125-5 kg/ha, almost complete destruction of weeds is achieved in the absence of phytotoxicity in relation to cultivated plants, for example, rice. 2 tab. CO s
Description
Изобретение относитс к химическим способам борьбы с сорной и нежелательной растительностью.This invention relates to chemical methods for controlling weeds and unwanted vegetation.
Целью изобретени вл етс повышение гербицидного действи .The aim of the invention is to increase the herbicidal effect.
Активные вещества, используемые в предложенном способе, представлены в табл . 1 ,The active substances used in the proposed method are presented in table. one ,
Активные вещества используют в дозах 0,3125-5 кг/га. Они могут использоватьс в виде обычных препара- тирных форм, например смачивающихс порошков, гранул, эмульгирующихс концентратов.The active substances are used in doses of 0.3125-5 kg / ha. They can be used in the form of conventional formulation forms, for example, wettable powders, granules, emulsifiable concentrates.
Пример 1. Специальные горшки наполн ли почвой с затопленного рисового пол и высаживали в них растени риса в стадии двух листьев, семена сорных растений (куриного проса , зонтичных, тростникового проса) и клубни балотницы. После этого г.орш- ки поставили в воду глубиной 3 см и на третий день после прорастани сорн ков почву обрабатывали смачивающим- 25 тем, что, с целью повьш1ени тербиExample 1. Special pots were filled with soil from a flooded rice floor and rice plants were planted in the two-leaf stage, weed seeds (chicken millet, umbrella millet, reed millet), and basil tuber. After that, the trees were put into the water with a depth of 3 cm and on the third day after weed germination, the soil was treated with a wetting-25 in order to increase the terbi
повреждение, остальные значени показателей промежуточные.damage, the remaining values of the indicators are intermediate.
Дл сравнени использовали известные гербициды: 6 -метилфенилацетани- лид (соединение А) и «6 , об-диметил- фенилацето-З-пропиланилид (соединение Б) .For comparison, known herbicides were used: 6-methylphenylacetanilide (compound A) and "6, dimethyl-phenylaceto-3-propylanilide (compound B).
Результаты опытов представлены в табл. 2 (номера соединений соответствуют номерам в табл. 1).The results of the experiments are presented in table. 2 (the numbers of the compounds correspond to the numbers in Table 1).
Полученные результаты свидетельствуют о высокой эффективности предло- женного способа и о его преимуществах перед известными способами-аналогами .The results obtained testify to the high efficiency of the proposed method and its advantages over the known analogous methods.
Форму л а изобретени Formula of invention
Способ борьбы с сорн ками путем обработки их или почвы, на которой они произрастают, производными фенил- ацетанилида, отличающийс A method of controlling weeds by treating them or the soil on which they grow is derived from phenyl acetanilide,
с порошком действующих веществ. Оценку гербицидного эффекта оценивали через 3 нед. после обработки по шкале 0-5 баллов: 5 - полна гибель растений; 4 - 80-99% поражени ; 3 - 6 0-79% поражени ; 2 - 40-52% поражени ; 1 - 20-39% поражени ; О - отсутствие повреждений.with powder active ingredients. Evaluation of the herbicidal effect was evaluated after 3 weeks. after processing on a scale of 0-5 points: 5 - the death of plants is full; 4 - 80-99% lesion; 3–6 0–79% lesion; 2 - 40-52% of the lesion; 1 - 20-39% of the lesion; O - no damage.
Фитотоксичность риса оценивали визуально по индексу: -, +, +, ++, +++, где (-) означает отсутствие фитоток- сичности, а (+++) означает Phytotoxicity of rice was evaluated visually by the index: -, +, +, ++, +++, where (-) means the absence of phytotoxicity, and (+++) means
00
5 five
цидного действи в качестве производного фенилацетанилида используют соединение общей формулыcidic action as a derivative of phenylacetanilide use a compound of general formula
ШгО т.SgO t.
I о II у1лI o II u1l
ИAND
YY
С- WITH-
где У - метил, метилокси, пропилокси,where Y is methyl, methyloxy, propyloxy,
трифторметил или фтор; R - С -С -алкил, в количестве 0,3125-5 кг/га.trifluoromethyl or fluorine; R - C-C-alkyl, in the amount of 0.3125-5 kg / ha.
Таблица Активные вещества общей формулыTable Active compounds of general formula
YY
СН-ь C-CCOINH- OyCH C-CCOINH- Oy
Продолжение табл.1Continuation of table 1
Продолжение табл.2Continuation of table 2
Продолжение табл. 2Continued table. 2
13277801327780
10 Пр одолже н ие табл.210 Prevailing Table 2
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58244071A JPS60136546A (en) | 1983-12-26 | 1983-12-26 | Substituted phenylacetanilide derivative, its production and use thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
SU1327780A3 true SU1327780A3 (en) | 1987-07-30 |
Family
ID=17113296
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU843831924A SU1327780A3 (en) | 1983-12-26 | 1984-12-25 | Method of fighting weeds |
Country Status (8)
Country | Link |
---|---|
US (1) | US4685962A (en) |
EP (1) | EP0147788B1 (en) |
JP (1) | JPS60136546A (en) |
KR (1) | KR910002672B1 (en) |
AT (1) | ATE53833T1 (en) |
BR (1) | BR8406690A (en) |
DE (1) | DE3482109D1 (en) |
SU (1) | SU1327780A3 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0565258A (en) * | 1991-07-03 | 1993-03-19 | Nippon Bayeragrochem Kk | Acetic acid anilide derivative and herbicide |
JP7221064B2 (en) | 2019-01-30 | 2023-02-13 | 太陽インキ製造株式会社 | Dry films, cured products and electronic components |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1101711A (en) * | 1964-01-23 | 1968-01-31 | Bellon Labor Sa Roger | New amides |
JPS55104240A (en) * | 1979-02-07 | 1980-08-09 | Idemitsu Kosan Co Ltd | N-(alpha,alpha-dimethylbenzyl)-acetamide derivative and herbicide containing the same |
JPS55162757A (en) * | 1979-06-05 | 1980-12-18 | Ihara Chem Ind Co Ltd | Meta-trifluoromethylphenylacetanilide and herbicide contaning it as active constituent |
JPS56108752A (en) * | 1980-01-28 | 1981-08-28 | Sumitomo Chem Co Ltd | N-substituted benzylphenylacetamide derivative, its preparation and herbicide containing the same as active constituent |
NZ197008A (en) * | 1980-05-22 | 1984-10-19 | Ici Ltd | Acylanilide derivatives and pharmaceutical compositions |
JPS599521B2 (en) * | 1981-03-03 | 1984-03-03 | 八洲化学工業株式会社 | herbicide |
JPS5843943A (en) * | 1982-08-09 | 1983-03-14 | Idemitsu Kosan Co Ltd | N-(alpha,alpha-dimethylbenzyl)phenylacetamide derivative and herbicide containing the same |
JPS6023105B2 (en) * | 1982-10-22 | 1985-06-05 | 八洲化学工業株式会社 | α,α-dimethylphenylacetic acid anilide derivative, its production method and herbicide containing the same |
JPS5979045A (en) * | 1982-10-28 | 1984-05-08 | Honda Motor Co Ltd | V-type engine |
JPS6023106B2 (en) * | 1983-01-17 | 1985-06-05 | 八洲化学工業株式会社 | α-Methyl-α-ethylphenyl acetic acid anilide derivative, its production method and herbicide containing the same |
US4536346A (en) * | 1983-05-06 | 1985-08-20 | American Cyanamid Company | Aralkanamidophenyl compounds |
JPS6023107B2 (en) * | 1983-07-25 | 1985-06-05 | 八洲化学工業株式会社 | α,α-dimethylphenylacetic acid anilide derivative, its production method and herbicide containing the same |
-
1983
- 1983-12-26 JP JP58244071A patent/JPS60136546A/en active Granted
-
1984
- 1984-12-17 US US06/682,762 patent/US4685962A/en not_active Expired - Lifetime
- 1984-12-19 EP EP84115855A patent/EP0147788B1/en not_active Expired - Lifetime
- 1984-12-19 AT AT84115855T patent/ATE53833T1/en not_active IP Right Cessation
- 1984-12-19 DE DE8484115855T patent/DE3482109D1/en not_active Expired - Fee Related
- 1984-12-21 BR BR8406690A patent/BR8406690A/en unknown
- 1984-12-25 SU SU843831924A patent/SU1327780A3/en active
- 1984-12-26 KR KR1019840008367A patent/KR910002672B1/en not_active IP Right Cessation
Non-Patent Citations (1)
Title |
---|
Chemical Abstracts, vol. 85. * |
Also Published As
Publication number | Publication date |
---|---|
EP0147788A2 (en) | 1985-07-10 |
JPS6353184B2 (en) | 1988-10-21 |
ATE53833T1 (en) | 1990-06-15 |
US4685962A (en) | 1987-08-11 |
EP0147788A3 (en) | 1986-06-25 |
KR850004583A (en) | 1985-07-25 |
BR8406690A (en) | 1985-10-22 |
DE3482109D1 (en) | 1990-06-07 |
EP0147788B1 (en) | 1990-05-02 |
JPS60136546A (en) | 1985-07-20 |
KR910002672B1 (en) | 1991-05-03 |
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